Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356664014 | Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 626779017 | Lysosomal alpha-1,4-glucosidase deficiency - infantile onset (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | localisation d'une constatation (attribut) | structure de muscle squelettique | false | Inferred relationship | Some | ||
| Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | localisation d'une constatation (attribut) | foie | false | Inferred relationship | Some | ||
| Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Lysosomal alpha-1,4-glucosidase deficiency - infantile onset | est un(e) (attribut) | Glycogen storage disease type II | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR